A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272399



Internal ID20839439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136704557..136706268hg38UCSC Ensembl
chr6:137025695..137027406hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg381712
hg191712
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567717
Supporting Variants
Samples
Known GenesMAP3K5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272399
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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